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产前糖皮质激素暴露导致前额叶皮层基因转录出现性别特异性和跨代变化,与行为结果相关。

Antenatal Glucocorticoid Exposure Results in Sex-Specific and Transgenerational Changes in Prefrontal Cortex Gene Transcription that Relate to Behavioural Outcomes.

机构信息

Departments of Physiology, University of Toronto, Toronto, ON, M5S1A8, Canada.

Departments of Pharmacology & Therapeutics, Sackler Program for Epigenetics & Psychobiology, McGill University, Montreal, QC, H3G1Y6, Canada.

出版信息

Sci Rep. 2019 Jan 24;9(1):764. doi: 10.1038/s41598-018-37088-3.

Abstract

Synthetic glucocorticoids (sGC) are administered to women at risk for pre-term delivery to reduce respiratory distress syndrome in the newborn. The prefrontal cortex (PFC) is important in regulating stress responses and related behaviours and expresses high levels of glucocorticoid receptors (GR). Further, antenatal exposure to sGC results in a hyperactive phenotype in first generation (F) juvenile male and female offspring, as well as F and F juvenile females from the paternal lineage. We hypothesized that multiple courses of antenatal sGC modify gene expression in the PFC, that these effects are sex-specific and maintained across multiple generations, and that the gene sets affected relate to modified locomotor activity. We performed RNA sequencing on PFC of F juvenile males and females, as well as F and F juvenile females from the paternal lineage and used regression modelling to relate gene expression and behavior. Antenatal sGC resulted in sex-specific and generation-specific changes in gene expression. Further, the expression of 4 genes (C9orf116, Calb1, Glra3, and Gpr52) explained 20-29% of the observed variability in locomotor activity. Antenatal exposure to sGC profoundly influences the developing PFC; effects are evident across multiple generations and may drive altered behavioural phenotypes.

摘要

合成糖皮质激素(sGC)被用于有早产风险的妇女,以减少新生儿呼吸窘迫综合征。前额皮质(PFC)在调节应激反应和相关行为方面起着重要作用,并表达高水平的糖皮质激素受体(GR)。此外,产前暴露于 sGC 会导致第一代(F1)雄性和雌性幼崽以及来自父系的 F1 和 F2 雌性幼崽表现出过度活跃的表型。我们假设多次产前 sGC 会改变 PFC 中的基因表达,这些影响具有性别特异性,并在多个世代中保持,并且受影响的基因集与运动活动的改变有关。我们对 F1 雄性和雌性幼崽以及来自父系的 F1 和 F2 雌性幼崽的 PFC 进行了 RNA 测序,并使用回归模型来关联基因表达和行为。产前 sGC 导致基因表达的性别特异性和世代特异性变化。此外,4 个基因(C9orf116、Calb1、Glra3 和 Gpr52)的表达解释了运动活动观察到的变异性的 20-29%。产前暴露于 sGC 会严重影响发育中的 PFC;这些影响在多个世代中都很明显,可能导致行为表型改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e9/6346022/a1c09e6f515f/41598_2018_37088_Fig2_HTML.jpg

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